Effectiveness of the Cytokine Hemadsorption on Sepsis
Completed
- Conditions
- Interleukin-6
- Registration Number
- NCT05057455
- Lead Sponsor
- Biruni University
- Brief Summary
In this prospective study, we aimed to compare the laboratory and clinical results of cytokine hemadsorption as an immunomodulation therapy in ICU patients diagnosed with sepsis or septic shock.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 39
Inclusion Criteria
- the patients were the available data of clinical and laboratory diagnosis of sepsis and septic shock
- detection of gram-negative bacterial agent in blood or sputum culture.
- patients who had the shock symptoms such as hypotension, tachycardia or fever during the course of sepsis.
Exclusion Criteria
- had uncontrolled hemorrhage,
- diagnosed with cardiac failure at stage 4 or renal failure at stage 4 or hepatic liver failure at stage 4
- cancer at the end stage or admitted with acute coronary syndrome.
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method IL-6 1 YEARS levels of IL-6
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular mechanisms underlie cytokine hemadsorption in sepsis immunomodulation?
How does cytokine hemadsorption compare to standard-of-care treatments for septic shock outcomes?
Which biomarkers correlate with improved survival in sepsis patients undergoing cytokine hemadsorption?
What adverse events are associated with cytokine hemadsorption in ICU sepsis patients?
Are there combination therapies that enhance cytokine hemadsorption efficacy in sepsis?
Trial Locations
- Locations (1)
Ilke Kupeli
🇹🇷Istanbul, Turkey
Ilke Kupeli🇹🇷Istanbul, Turkey